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HRID2114497

反应详情

EQUATION

反应方程式

HRID 2114497 的结构方程式

REACTANTS

反应物

4
反应SMILES：Oc1ccccc1Br
HCID7244

2-Bromophenol

C6H5BrO

反应SMILES：COc1cccc(F)c1[N+](=O)[O-]
HCID2782776

3-Fluoro-2-nitroanisole

C7H6FNO3

反应SMILES：N#Cc1ccc([N+](=O)[O-])c(F)c1
HCID2783399

3-Fluoro-4-nitrobenzonitrile

C7H3FN2O2

反应SMILES：COC(=O)c1ccc(NC2CCN(Cc3ccccc3)CC2)c(O)c1
HCID59809567

未命名化合物

PRODUCTS

产物

1
反应SMILES：COC(=O)c1ccc2c(c1)Oc1c(OC)cccc1N2C1CCN(Cc2ccccc2)CC1
HCID59809540

未命名化合物

PROCEDURE

实验过程

Using an adaptation of the method described in Procedure 1, substituting 4-(1-benzyl-piperidin-4-ylamino)-3-hydroxy-benzoic acid methyl ester, 1d for 2-bromophenol, and 1-fluoro-3-methoxy-2-nitrobenzene for 3-fluoro-4-nitrobenzonitrile, the title compound 10-(1-benzyl-piperidin-4-yl)-6-methoxy-10H-phenoxazine-3-carboxylic acid methyl ester, 2d was obtained.